JP2009203446A - Adhesive composition for capturing small creature - Google Patents

Adhesive composition for capturing small creature Download PDF

Info

Publication number
JP2009203446A
JP2009203446A JP2008050228A JP2008050228A JP2009203446A JP 2009203446 A JP2009203446 A JP 2009203446A JP 2008050228 A JP2008050228 A JP 2008050228A JP 2008050228 A JP2008050228 A JP 2008050228A JP 2009203446 A JP2009203446 A JP 2009203446A
Authority
JP
Japan
Prior art keywords
mass
adhesive composition
composition
polybutene
adhesive
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2008050228A
Other languages
Japanese (ja)
Inventor
Ryoji Ida
領二 伊田
Yoshihiro Goshi
義広 合志
Koichi Sato
浩一 佐藤
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eneos Corp
Original Assignee
Nippon Oil Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Oil Corp filed Critical Nippon Oil Corp
Priority to JP2008050228A priority Critical patent/JP2009203446A/en
Priority to TW098104822A priority patent/TWI449764B/en
Priority to PCT/JP2009/053467 priority patent/WO2009107687A1/en
Priority to CN2009801066484A priority patent/CN101959986B/en
Publication of JP2009203446A publication Critical patent/JP2009203446A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J123/00Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers
    • C09J123/02Adhesives based on homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Adhesives based on derivatives of such polymers not modified by chemical after-treatment
    • C09J123/18Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
    • C09J123/20Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04Homopolymers or copolymers of ethene
    • C08L23/06Polyethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/18Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
    • C08L23/20Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
    • C08L23/22Copolymers of isobutene; Butyl rubber ; Homo- or copolymers of other iso-olefins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Catching Or Destruction (AREA)
  • Paints Or Removers (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide an adhesive composition for capturing small creatures which has a good adhesive power, is easy to handle as a coating to be applied into a material to be coated, is made of a raw material which is easily obtainable, and has excellent workability when made into an adhesive composition. <P>SOLUTION: A composition comprising (A) 70-98 mass% of a liquid state polybutene having a number-average molecular weight of 200-1200, (B) 1.0-8.0 mass% of a high pressure produced-polyethylene having a melt index of 0.04-35, (C) 1.0-8.0 mass% of a butyl rubber having a Mooney viscosity ML<SB>1+8</SB>(125°C) of 30-60, and (D) 5-29 mass% of an alicyclic hydrocarbon resin constitutes an adhesive composition for capturing small creatures. <P>COPYRIGHT: (C)2009,JPO&INPIT

Description

本発明は、ネズミ、ゴキブリ、ハエ等の小生物を捕獲するのに適した粘着性組成物に関する。   The present invention relates to an adhesive composition suitable for capturing small organisms such as mice, cockroaches and flies.

ネズミ、ゴキブリ、ハエ等の有害小生物の駆除は生活環境の改善面から重要な課題である。特にげっ歯類による被害は膨大なものであり、中でもネズミは、農産物、食品はもちろんのこと、鉛管を食い破ってガス漏洩を起こしたり、電灯線を露出させ火災を起こすこともある。これらの小生物の駆除方法として従来からいくつかのものが提案され実施されているが、それらの中で最も簡便なものとして、粘着性を有する捕獲剤を厚紙、ボール紙、木板、プラスチックフイルム、シートなどの被塗布材料に塗布し、小生物の通路に設置する方法がある。この場合、捕獲剤は塗布作業性にすぐれかつ粘着性にもすぐれているという要請を満たさなければならない。さらに、あらかじめ被塗布材料に塗布しておく場合などには、保存中又はこれを使用中に捕獲剤が被塗布材料から流れ出したり、あるいは被塗布材料に浸透してにじみ出したりして使用不能になったり床を汚すようなことがあってはならない。   Exterminating harmful small organisms such as rats, cockroaches and flies is an important issue from the viewpoint of improving the living environment. In particular, the damage caused by rodents is enormous. Among them, rats can eat not only agricultural products and food, but also break the lead pipe to cause gas leakage, or expose the power line to cause a fire. Several methods for extermination of these small organisms have been proposed and implemented, but the simplest of them is a sticky capture agent such as cardboard, cardboard, wood board, plastic film, There is a method in which it is applied to a material to be applied such as a sheet and installed in a passage for small organisms. In this case, it is necessary to satisfy the requirement that the capture agent is excellent in application workability and adhesiveness. In addition, when pre-applied to the material to be coated, the trapping agent flows out of the material to be coated during storage or use, or penetrates into the material to be spread and becomes unusable. There should be no such things as becoming dirty or soiling the floor.

この種の小生物捕獲剤としては、例えばポリブテン86 %、ブチルゴム10 %およびたれ防止剤としてのパラフイン4 %より成る組成物(特許文献1)、ポリブテン80部、ブチルゴム10 部およびロジン、シリカゲル、ポリエチレン計40部より成る組成物(特許文献2)、ポリイソブテン(50℃ における粘度が1000ポイズ)またはポリイソブテンと天然ゴムとの80:20混合物100質量部に対し、それぞれ有機ベントナイト2〜40質量部あるいはコロイダルシリカ0.5〜8質量部を配合した組成物(特許文献3、特許文献4)、またブチルゴム5 質量%、ポリブテン35質量%、およびロジンエステル、トルエン、キシレン計60質量%より成る組成物(特許文献5)などが開示されている。また、ポリブテン80質量%、ブチルゴム16質量%およびポリエチレン4質量%からなる組成物(特許文献6)、さらには、分子量が異なる二種類の液状ポリブテンの混合物80〜98質量%、粘度平均分子量が100万〜250万のポリイソブチレンゴム1〜10質量%、特定の性状を有する高圧法ポリエチレン1〜10質量%からなる組成物が開示されている(特許文献7)。   As this kind of small organism capture agent, for example, a composition comprising 86% polybutene, 10% butyl rubber and 4% paraffin as an anti-sagging agent (Patent Document 1), 80 parts polybutene, 10 parts butyl rubber and rosin, silica gel, polyethylene 2 to 40 parts by weight of organic bentonite or colloidal to 100 parts by weight of a composition comprising 40 parts in total (Patent Document 2), polyisobutene (viscosity of 1000 poise at 50 ° C.) or 80:20 mixture of polyisobutene and natural rubber, respectively A composition comprising 0.5 to 8 parts by mass of silica (Patent Documents 3 and 4), a composition comprising 5% by mass of butyl rubber, 35% by mass of polybutene, and 60% by mass of rosin ester, toluene, and xylene. Patent document 5) etc. are disclosed. Further, a composition comprising 80% by mass of polybutene, 16% by mass of butyl rubber and 4% by mass of polyethylene (Patent Document 6), a mixture of two kinds of liquid polybutenes having different molecular weights, 80 to 98% by mass, and a viscosity average molecular weight of 100 A composition comprising 1 to 10% by mass of 10,000 to 2.5 million polyisobutylene rubber and 1 to 10% by mass of high-pressure polyethylene having specific properties is disclosed (Patent Document 7).

しかし、これらの例は、いずれも前記の要請のすべてを満たすものではない。具体的には、パラフインワツクスを用いた組成物においては、少量の添加では流れ出し防止効果が十分でなく、一方十分な量を添加すれば、塗布後の時間経過とともに、ワックス分が粘着層の表面に移動し、粘着力を低下させるため、捕獲能力が著しく低下する。高価な有機ベントナイトあるいはシリカを用いた組成物においては、比較的流れ出し防止効果や粘着力の面で良好であるが、これら粉状物は嵩高く混合時に空気を巻込んで、混合後の脱泡など製造時の手間あるいはコストの面から好ましくない。
また、ブチルゴム、ポリブテン、およびロジンエステル、トルエン、キシレンより成る組成物は揮発性の芳香族溶剤を使用するため臭気の問題がある。さらには当該粘着性組成物を塗布した塗膜を小生物捕獲用に設置して長時間経過中に溶剤が揮散し、塗布膜が硬化し、捕獲能力が低下する問題も避けられない。また、ポリブテン、ブチルゴムおよびポリエチレンからなる組成物は粘着性組成物の粘着性と塗布作業時の作業性の双方を満足させることは出来ない。
また、特開昭2007−177104で開示されている、ポリイソブチレンゴムを用いるものは、粘着力は優れているものの、ポリイソブチレンゴムの分子量が非常に大きいため、混練してポリブテンに溶解するのに時間がかかるという欠点を有する。また、ポリイソブチレンゴムは供給元が限られ、高価な上に安定供給に問題がある。また、2種類の液状ポリブテンを用いるなど、作業上の手間も大きい。
特公昭48−16617号公報 特開昭52−105217号公報 特開昭51−125123号公報 特公昭53−18586号公報 特開昭52−98161号公報 特公平2−57521号公報 特開昭2007−177104号公報
However, none of these examples meet all of the above requirements. Specifically, in a composition using paraffin wax, the addition of a small amount is not sufficient to prevent the flow-out, whereas if a sufficient amount is added, the wax content of the adhesive layer increases with the passage of time after application. Since it moves to the surface and reduces the adhesive force, the capture ability is significantly reduced. In the composition using expensive organic bentonite or silica, it is relatively good in terms of prevention of flow-out and adhesive strength. However, these powders are bulky and involve air during mixing, and defoamed after mixing. This is not preferable from the viewpoint of labor and cost during production.
Further, a composition comprising butyl rubber, polybutene, rosin ester, toluene, and xylene has a problem of odor because it uses a volatile aromatic solvent. Furthermore, the problem is that the coating film coated with the adhesive composition is installed for capturing small organisms, the solvent is volatilized over a long period of time, the coating film is cured, and the capturing ability is lowered. Further, a composition comprising polybutene, butyl rubber and polyethylene cannot satisfy both the tackiness of the tacky composition and the workability during the coating operation.
Also, those using polyisobutylene rubber disclosed in JP-A-2007-177104 have excellent adhesion, but the molecular weight of polyisobutylene rubber is very large, so that it is kneaded and dissolved in polybutene. It has the disadvantage of taking time. Polyisobutylene rubber has a limited supply source and is expensive and has a problem in stable supply. In addition, it requires a lot of work, such as using two types of liquid polybutene.
Japanese Patent Publication No. 48-16617 JP-A-52-105217 JP 51-125123 A Japanese Patent Publication No.53-18586 JP 52-98161 A Japanese Examined Patent Publication No. 2-57521 JP 2007-177104 A

本発明の課題は、小生物捕獲用の粘着性に優れ、粘着性組成物の製造時あるいは製造された粘着性組成物の塗布作業時の作業性に優れ、さらには、塗布後の粘着性組成物の流れ出しが無い、などの諸要請に応える優れた性能を有し、しかも原材料の入手が容易で且つ安価な小生物捕獲用粘着性組成物を提供することにある。   The object of the present invention is excellent in tackiness for capturing small organisms, excellent in workability during the production of the adhesive composition or during the application of the produced adhesive composition, and moreover, the adhesive composition after application It is an object of the present invention to provide an adhesive composition for capturing small organisms that has excellent performance in response to various requests such as the absence of a material flow, and that is easy to obtain raw materials and is inexpensive.

本発明は、
(A)数平均分子量200 〜1200の液状ポリブテン70〜98質量%、および
(B)メルトインデックスが0.04 〜35の高圧法ポリエチレン1.0〜8.0質量%、
(C)ムーニー粘度ML1+8(125℃)30〜60のブチルゴム1.0〜8.0質量%、および
(D)脂環式炭化水素樹脂5〜29質量%より成る(全体を100質量%とする)ことを特徴とする小生物捕獲用粘着性組成物に関するものである。
The present invention
(A) 70-98% by mass of liquid polybutene having a number average molecular weight of 200-1200, and (B) 1.0-8.0% by mass of high-pressure polyethylene having a melt index of 0.04-35,
(C) Mooney viscosity ML 1 + 8 (125 ° C.) 30 to 60 butyl rubber 1.0 to 8.0 mass%, and (D) alicyclic hydrocarbon resin 5 to 29 mass% (total 100 mass) %). The present invention relates to an adhesive composition for capturing small organisms.

本発明によれば、液状ポリブテン、ポリエチレン、ブチルゴムからなる組成物にさらに脂環式炭化水素樹脂を加えることにより、従来のポリブテン、ポリエチレン、ブチルゴム、ロジンあるいはシリカゲルからなる組成物と比較して、小生物に対する粘着性に優れ、製造時の作業性および粘着性組成物の塗布作業の作業性等に優れ、さらには塗布後の粘着性組成物の流れ出しなどの欠点の無い、安価で且つ優れた性能を有する小生物捕獲用粘着性組成物を提供できる。   According to the present invention, by adding an alicyclic hydrocarbon resin to a composition comprising liquid polybutene, polyethylene, and butyl rubber, compared with a composition comprising conventional polybutene, polyethylene, butyl rubber, rosin, or silica gel, Excellent adhesiveness to living organisms, excellent workability at the time of manufacture and workability of the adhesive composition application work, etc., and low cost and excellent performance without any drawbacks such as the flow of adhesive composition after application An adhesive composition for capturing small organisms can be provided.

以下、本発明について更に詳しく述べる。
本発明で用いる(A)液状ポリブテンは、数平均分子量が200 〜1200の範囲のものである。さらに好ましい数平均分子量の範囲は400〜1200のものである。この液状ポリブテンは例えばナフサ分解により生成するいわゆるC4留分のうちブタジエンを除いたブタン−ブテン留分を重合することにより製造できる。これらのポリブテンは、例えば日石ポリブテン(新日本石油(株))の商品名で市販されている。ポリブテンの数平均分子量が200より小さい場合には、引火点が低くなるため、本粘着性組成物の製造時もしくは調理場等の火気のある所で使用する際の安全性が低下する。また、得られた粘着性組成物の粘着力が低下するため好ましくない。また数平均分子量が1200より大きい場合には、粘着性組成物の溶融粘度が大きくなりすぎるため、円滑な塗布作業が不可能となる。
Hereinafter, the present invention will be described in more detail.
The liquid polybutene (A) used in the present invention has a number average molecular weight in the range of 200 to 1200. A more preferred number average molecular weight range is 400-1200. This liquid polybutene can be produced, for example, by polymerizing a butane-butene fraction excluding butadiene in a so-called C4 fraction produced by naphtha decomposition. These polybutenes are commercially available, for example, under the trade name Nisseki Polybutene (Shin Nippon Oil Co., Ltd.). When the number average molecular weight of the polybutene is smaller than 200, the flash point becomes low, so that the safety when the present adhesive composition is produced or used in a place with a fire such as a cooking place is lowered. Moreover, since the adhesive force of the obtained adhesive composition falls, it is not preferable. On the other hand, if the number average molecular weight is larger than 1200, the melt viscosity of the pressure-sensitive adhesive composition becomes too high, and a smooth coating operation is impossible.

高圧法ポリエチレンとは、エチレン単独又はエチレンと他のオレフィン(例えば、ブテン、ペンテン、ヘキセン等)を高圧重合法において重合したものであり、密度が0.92〜0.93のものを意味する。本発明で用いる(B)高圧法ポリエチレンは、メルトインデックスが0.04〜35、好ましくは0.1〜20のものである。メルトインデックスが0.04より小さいものは液状ポリブテンへの溶解に高い温度と長時間を要し、またこの範囲より大きいものは粘着性、捕獲剤の流れ出し防止効果およびにじみ出し防止効果の十分なものは得られない。高圧法ポリエチレンは例えば、商品名ノバテックLJ600(日本ポリエチレン(株))を入手して使用することが出来る。高圧法ポリエチレンは単独でも複数使用してもよい。   The high-pressure polyethylene means a polymer obtained by polymerizing ethylene alone or ethylene and another olefin (for example, butene, pentene, hexene, etc.) in a high-pressure polymerization method, and having a density of 0.92 to 0.93. The high-pressure polyethylene (B) used in the present invention has a melt index of 0.04 to 35, preferably 0.1 to 20. Those with a melt index less than 0.04 require a high temperature and a long time for dissolution in liquid polybutene, and those with a melt index greater than this range are sufficient in tackiness, capture agent flow prevention effect and bleeding prevention effect. Cannot be obtained. The high-pressure polyethylene can be obtained by using, for example, the trade name Novatec LJ600 (Nippon Polyethylene Co., Ltd.). The high pressure polyethylene may be used alone or in combination.

本発明で用いる(C) ブチルゴムとはムーニー粘度ML1+8(125℃)30〜60、好ましくは45〜55のブチルゴムである。これらのブチルゴムは例えば、BUTYL268(JSR(株)製)の商品名で市販されている。ムーニー粘度ML1+8(125℃)が30より小さい場合には製造された粘着性組成物の粘着力が不十分であり、小生物に対する捕獲性が低下する。一方、60より大きい場合はポリブテンに対する溶解に時間が掛かりまた製造された粘着性組成物の溶融粘度が非常に高粘度となるため被塗布材料面に円滑に塗布することが困難となる。 The (C) butyl rubber used in the present invention is butyl rubber having a Mooney viscosity ML 1 + 8 (125 ° C.) of 30 to 60, preferably 45 to 55. These butyl rubbers are commercially available, for example, under the trade name BUTYL268 (manufactured by JSR Corporation). When Mooney viscosity ML1 + 8 (125 degreeC) is smaller than 30, the adhesive force of the manufactured adhesive composition is inadequate, and the capture property with respect to a small organism falls. On the other hand, when it is larger than 60, it takes time to dissolve in polybutene, and the melt viscosity of the produced pressure-sensitive adhesive composition becomes very high, so that it is difficult to smoothly apply to the surface of the material to be coated.

本発明に用いる(D)脂環式炭化水素樹脂とはシクロペンタジエンあるいはアルキルシクロペンタジエンの如き脂環式オレフィン系化合物を、酸触媒を用いて重合して得た樹脂或いはアルケニル芳香族炭化水素を酸触媒を用いて重合した後、芳香環を核水素化して得た樹脂などが挙げられる。これらの脂環式炭化水素樹脂は例えば商品名Escorez5300(Exxon Mobil Chemical社製)として市場から入手できる。   The (D) alicyclic hydrocarbon resin used in the present invention is a resin or alkenyl aromatic hydrocarbon obtained by polymerizing an alicyclic olefin compound such as cyclopentadiene or alkylcyclopentadiene using an acid catalyst. Examples thereof include resins obtained by polymerization using a catalyst and then nuclear hydrogenation of an aromatic ring. These alicyclic hydrocarbon resins are commercially available, for example, under the trade name Escorez 5300 (manufactured by Exxon Mobile Chemical).

本発明における液状ポリブテンの配合割合は、組成物全体に対して70〜98質量%、好ましくは75〜85質量%である。液状ポリブテンの配合割合が70質量%よりも少ないと塗布膜の伸展性が低下し、表面の凹凸の生成等、塗布加工性に劣る傾向にある。また、98質量%よりも大きいと塗布膜の耐流れ出し性に劣る傾向にある。   The blending ratio of the liquid polybutene in the present invention is 70 to 98% by mass, preferably 75 to 85% by mass with respect to the entire composition. If the blending ratio of the liquid polybutene is less than 70% by mass, the extensibility of the coating film is lowered and the coating processability tends to be inferior, such as generation of surface irregularities. On the other hand, if it exceeds 98% by mass, the flow resistance of the coating film tends to be inferior.

本発明における高圧法ポリエチレンの配合割合は組成物全体に対して1.0〜8.0質量%、好ましくは2.0〜6.0質量%、さらに好ましくは3.0〜4.5質量%の範囲である。配合割合が1.0質量%よりも小さいと、塗布膜の耐流れ出し性が劣る。一方8.0質量%よりも大きいと、塗膜形成性が低下し、表面の凹凸の生成等、塗布膜の加工性に劣る。   The blending ratio of the high pressure polyethylene in the present invention is 1.0 to 8.0% by mass, preferably 2.0 to 6.0% by mass, more preferably 3.0 to 4.5% by mass, based on the entire composition. Range. When the blending ratio is less than 1.0% by mass, the flow-out resistance of the coating film is inferior. On the other hand, when it is larger than 8.0% by mass, the coating film formability is deteriorated and the processability of the coating film is inferior, such as the formation of surface irregularities.

ブチルゴムの配合割合は組成物全体に対して1.0〜8.0質量%、好ましくは2.0〜6.0質量%、さらに好ましくは2.5〜4.5質量%の範囲である。配合割合が1.0質量%よりも小さいと、粘着力が十分に得られず、また8.0質量%よりも大きいと、溶融粘度が極めて大きくなり塗布時の加工性に劣る。   The blending ratio of butyl rubber is 1.0 to 8.0% by mass, preferably 2.0 to 6.0% by mass, and more preferably 2.5 to 4.5% by mass with respect to the entire composition. When the blending ratio is less than 1.0% by mass, sufficient adhesive strength cannot be obtained, and when it is greater than 8.0% by mass, the melt viscosity becomes extremely large and the processability at the time of coating is poor.

本発明においてはその構成成分として、上記3種の成分に加えて脂環式炭化水素樹脂を加えることが必要である。脂環式炭化水素樹脂を用いることにより、粘着力と塗布時の作業性の双方が優れた粘着性組成物を得ることが出来る。脂環式炭化水素樹脂を用いずに粘着性組成物を製造した場合、塗布時の作業性が優れた組成物を得ようとした場合、その組成物は粘着力に劣るものしか得られない。一方、脂環式炭化水素樹脂を用いずに粘着力が満足できる組成物を製造した場合、その組成物は溶融粘度が極めて大きく、塗布作業性の劣るものとなり、何れも本発明の目的とする、粘着力と塗布時の作業性の双方が優れた粘着性組成物は得られない。脂環式炭化水素樹脂の配合割合は組成物全体に対して5〜29質量%、好ましくは7〜20質量%、さらに好ましくは9〜15質量%の範囲である。配合割合が5質量%よりも小さいと粘着性組成物の溶融粘度が高くなりすぎ、塗布性に問題が生じ、29質量%よりも大きいと溶融粘度が低くなりすぎ、その結果粘着物の耐フロー性が劣り好ましくない。また、塗布膜の粘着力が低く、小生物の捕獲性能に問題が生ずる。   In the present invention, it is necessary to add an alicyclic hydrocarbon resin as a constituent component in addition to the above three components. By using an alicyclic hydrocarbon resin, it is possible to obtain a pressure-sensitive adhesive composition that is excellent in both adhesive strength and workability during coating. In the case where an adhesive composition is produced without using an alicyclic hydrocarbon resin, when trying to obtain a composition having excellent workability at the time of application, the composition is only inferior in adhesive strength. On the other hand, when a composition with satisfactory adhesive strength is produced without using an alicyclic hydrocarbon resin, the composition has an extremely large melt viscosity and is inferior in coating workability, both of which are the object of the present invention. An adhesive composition excellent in both adhesive strength and workability during application cannot be obtained. The blending ratio of the alicyclic hydrocarbon resin is from 5 to 29% by mass, preferably from 7 to 20% by mass, and more preferably from 9 to 15% by mass, based on the entire composition. If the blending ratio is less than 5% by mass, the melt viscosity of the pressure-sensitive adhesive composition becomes too high, resulting in problems in applicability, and if it exceeds 29% by mass, the melt viscosity becomes too low. Inferior property is not preferable. Moreover, the adhesive force of the coating film is low, which causes a problem in the capture performance of small organisms.

本発明の粘着性組成物は、(A)〜(D)成分を溶融混練することにより製造することが出来る。溶融混練する方法は特に限定されたものではなく、公知の方法を用いて行うことが出来る。例えば、(A)〜(D)の各成分が溶融する温度条件下に、混練機を用いて強制的に攪拌するなどの方法を用いることが出来る。練装置としては公知の攪拌翼付きの釜等が好ましく使用できる。
混練方法としては、例えば、主成分である液状ポリブテンを加熱しておいて、そこに他の成分を順次または同時に加えて、混練する方法が好ましい。この一連の作業を行うのに好ましい温度範囲は、160℃〜170℃である。作業時間は、数量に応じて適宜調整するが、5〜7時間が好ましい。
The pressure-sensitive adhesive composition of the present invention can be produced by melt-kneading the components (A) to (D). The method of melt kneading is not particularly limited, and can be performed using a known method. For example, a method of forcibly stirring using a kneader can be used under a temperature condition where the components (A) to (D) are melted. As mixing kneading device hook or the like with known stirring blade is preferably used.
As a kneading method, for example, a method is preferably used in which liquid polybutene as a main component is heated, and other components are added sequentially or simultaneously thereto. A preferable temperature range for performing this series of operations is 160 ° C to 170 ° C. The working time is appropriately adjusted according to the quantity, but is preferably 5 to 7 hours.

また、得られた粘着性組成物を基材に塗布する方法は、公知のドクターナイフ法、ドクターブレード法等がいずれも好ましく使用できる。塗布時の粘着性組成物の温度は、160℃〜170℃が好ましい。   In addition, as a method for applying the obtained adhesive composition to a substrate, any of the known doctor knife method, doctor blade method and the like can be preferably used. The temperature of the adhesive composition at the time of application is preferably 160 ° C to 170 ° C.

本発明の組成物は有機溶剤を用いないので特異な臭気を有しないから、ネズミが忌避することがないし、誘引剤の効果を阻害することもない。また、ベントナイトやシリカのような嵩高な充填剤を用いないので、混練作業中に泡立ちを生じて、製造作業の継続を困難にするという問題も無い。本発明の粘着性組成物は、ネズミ等のげっ歯類小生物の捕獲に有効であるのはもちろん、それ以外の例えばゴキブリ等の有害小生物の捕獲にも使用できる。
なお、本発明の粘着性組成物は、適用する用途に応じて、その要求性能を損なわない範囲において、上記必須構成成分の他、必要に応じてプロセス油、動植物油、高分子可塑剤、軟化剤、着色剤、酸化防止剤、老化防止剤、香料、誘引剤、飼料等を適宜配合することが出来る。
Since the composition of the present invention does not use an organic solvent and does not have a specific odor, mice are not repelled and the effect of the attractant is not inhibited. Further, since a bulky filler such as bentonite or silica is not used, there is no problem of causing foaming during the kneading operation and making it difficult to continue the manufacturing operation. The adhesive composition of the present invention is not only effective for capturing rodent small organisms such as mice, but also can be used for capturing other harmful small organisms such as cockroaches.
The pressure-sensitive adhesive composition of the present invention is a process oil, animal and vegetable oil, a polymer plasticizer, a softening agent, if necessary, in addition to the above essential constituents, within a range that does not impair the required performance depending on the application to be applied. An agent, a colorant, an antioxidant, an anti-aging agent, a fragrance, an attractant, a feed and the like can be appropriately blended.

以下、実施例により本発明を具体的に説明するが、本発明はこれらの実施例に限定されるものではない。   EXAMPLES Hereinafter, although an Example demonstrates this invention concretely, this invention is not limited to these Examples.

<実施例1〜3および比較例1〜6>
以下に示す材料を用いて、表1に示す配合割合にしたがって各種の粘着性組成物を調製した。
ブチルゴム;JSR社製 BUTYL268、ムーニー粘度ML1+8(125℃)51
ポリイソブチレンゴム;Exxon Mobil Chemical社製 Vistanex L-120、 重量平均分子量166万
高圧法ポリエチレン;日本ポリエチレン(株)製、ノバテックLJ600、MFR5.5、密度0.93、融点(DSC法)108℃
液状ポリブテンA;新日本石油化学(株)製、日石ポリブテンHV-100、数平均分子量980
液状ポリブテンB;新日本石油化学(株)製、日石ポリブテンHV-300、数平均分子量1400
脂環式炭化水素樹脂A;Exxon Mobil Chemical社製 Escorez5300、融点105℃
脂肪族炭化水素樹脂B;Exxon Mobil Chemical社製 Escorez1304、融点100℃
<Examples 1-3 and Comparative Examples 1-6>
Various adhesive compositions were prepared according to the blending ratios shown in Table 1 using the materials shown below.
Butyl rubber: JSR BUTYL268, Mooney viscosity ML 1 + 8 (125 ° C) 51
Polyisobutylene rubber: Vistanex L-120 manufactured by Exxon Mobil Chemical, weight average molecular weight 1.66 million high-pressure polyethylene; Nippon Polyethylene Corporation, Novatec LJ600, MFR5.5, density 0.93, melting point (DSC method) 108 ° C
Liquid polybutene A: Nippon Petrochemical Co., Ltd., Nisseki Polybutene HV-100, number average molecular weight 980
Liquid polybutene B: Nippon Petrochemical Co., Ltd., Nisseki Polybutene HV-300, number average molecular weight 1400
Alicyclic hydrocarbon resin A; Escorez 5300, Exxon Mobil Chemical Co., melting point 105 ° C
Aliphatic hydrocarbon resin B; Escorez 1304, Exxon Mobil Chemical Co., melting point 100 ° C

粘着性組成物の調製方法は以下のとおりである。すなわち、170℃に加熱した液状ポリブテンに、他の成分を逐次加えて、温度を170℃に保持して各成分が均一に溶解するまで攪拌した。比較例4は特開昭2007−177104で開示されている、ポリイソブチレンゴムを用いるもので、粘着力は優れているものであるが、ポリイソブチレンゴムの分子量が非常に大きいため、混練してポリブテンに溶解するのに他の例に比べて著しく長い時間がかかった。次に、これらの粘着性組成物の溶融粘度および粘着力の性能を評価した。評価結果を表1に示す。なお、評価方法は以下のとおりである。   The method for preparing the adhesive composition is as follows. That is, other components were sequentially added to the liquid polybutene heated to 170 ° C., and the temperature was maintained at 170 ° C. and stirred until each component was uniformly dissolved. Comparative Example 4 uses a polyisobutylene rubber disclosed in JP-A-2007-177104 and has excellent adhesive strength. However, since the molecular weight of the polyisobutylene rubber is very large, it is kneaded and mixed with polybutene. It took significantly longer time to dissolve in the sample than in the other examples. Next, the melt viscosity and adhesive strength performance of these adhesive compositions was evaluated. The evaluation results are shown in Table 1. The evaluation method is as follows.

<評価方法>
溶融粘度:JIS−K7117に準拠し、160℃に於ける溶融粘度を測定した。溶融粘度は粘着性組成物を被塗布面に塗布する際の作業性に影響する。表には溶融粘度の数値に加えて、塗布性能の評価も併記した。評価は以下のように行った。すなわち、170℃の粘着性組成物を、所定の寸法に打ち抜かれたステンレス製の型枠を用いて台紙の表面に厚さ2mmで塗布した。粘着性組成物が硬すぎず均一に塗布され、かつ塗布中あるいは塗布後の粘着性組成物の流れ出しも無かった(○)。粘着性組成物が硬すぎて均一に塗布することが難しかった(×)。塗布作業中あるいは塗布後の粘着性組成物の流れ出しが認められた(△)。
指触タック:塗布面に塗布した粘着性組成物表面に指を接触させ、指触タックを調べた。
評価 ×:指に殆ど付着しない。また、伸びが無くゴム弾性が無い。
△:指に付着するものの、ゴム弾性に欠ける。
○:指に付着し、かつ伸びがありゴム弾性がある。
粘着力:プローブタック法(JIS−Z0237補足事項)に準拠し、塗布面に塗布した粘着性組成物を直径5mmの金属柱の端面に接触させ、金属柱を塗布面から引き離すのに必要な力を23℃において引張試験機により測定した。粘着力は小生物の捕獲性能に影響する。
<Evaluation method>
Melt viscosity: The melt viscosity at 160 ° C. was measured according to JIS-K7117. The melt viscosity affects the workability when the adhesive composition is applied to the surface to be applied. In the table, in addition to the numerical value of the melt viscosity, the evaluation of the coating performance is also shown. Evaluation was performed as follows. That is, the adhesive composition at 170 ° C. was applied to the surface of the mount with a thickness of 2 mm using a stainless steel mold punched to a predetermined size. The adhesive composition was uniformly applied without being too hard, and the adhesive composition did not flow out during or after application (◯). The pressure-sensitive adhesive composition was too hard to apply uniformly (×). Flowing out of the adhesive composition during or after the coating operation was observed (Δ).
Finger touch tack: A finger was brought into contact with the surface of the pressure-sensitive adhesive composition coated on the coated surface, and the finger touch tack was examined.
Evaluation x: Almost no adhesion to fingers. Further, there is no elongation and no rubber elasticity.
Δ: Although it adheres to the finger, it lacks rubber elasticity.
○: Adhered to the finger, stretched and rubber elastic.
Adhesive strength: In accordance with the probe tack method (JIS-Z0237 supplementary matter), the force required to bring the adhesive composition applied to the coated surface into contact with the end surface of a metal column having a diameter of 5 mm and to pull the metal column away from the coated surface Was measured with a tensile tester at 23 ° C. Adhesive strength affects the capture performance of small organisms.

Figure 2009203446
Figure 2009203446

表1から明らかなように、液状ポリブテン、高圧法ポリエチレン、ブチルゴム、脂環式炭化水素樹脂からなる、実施例1〜3に示す本発明の粘着性組成物は、適切な溶融粘度を有し、指触タック、粘着力も良好である。すなわち小生物の捕獲性と塗布時の作業性双方に優れているものである。また、実施例1〜3を比較することにより、脂環式炭化水素樹脂の配合割合を調整することにより、所望の粘着力と溶融粘度に調整できることが分かる。   As is apparent from Table 1, the adhesive compositions of the present invention shown in Examples 1 to 3 comprising liquid polybutene, high-pressure polyethylene, butyl rubber, and alicyclic hydrocarbon resin have an appropriate melt viscosity, Good finger touch and adhesion. That is, it excels in both the capture of small organisms and the workability during application. Moreover, by comparing Examples 1-3, it turns out that it can adjust to desired adhesive force and melt viscosity by adjusting the mixture ratio of an alicyclic hydrocarbon resin.

これに対し、脂環式炭化水素樹脂を配合しない比較例1は塗布時の作業性は優れているが、粘着力に劣る。ブチルゴムの配合割合を大きくし、かつ、粘度が大きい液状ポリブテンを併用して粘着力を実施例1,2に合わせた比較例2では、粘着力は優れているが溶融粘度が大きく、塗布時の作業性に劣る。また、炭化水素樹脂として脂環式炭化水素樹脂の代わりに脂肪族炭化水素樹脂を用いた比較例3は、塗布時の作業性は優れているが、粘着力に劣る結果であり、樹脂B由来と思われる粘着物の臭気も強かった。比較例4は現在市販され、小生物捕獲用粘着性組成物として広く用いられているものであり、粘着力、塗布作業性ともに優れた実績を持つものである。表から明らかなように、実施例1、2および3は比較例4と比べて勝るとも劣らない粘着力と塗布作業性を有する。さらに、比較例4は本願のブチルゴムの代わりに超高分子のポリイソブチレンゴムを用いる。そのため、表1に示すように、混練作業時において混練物が均一になるまでの時間が長く、粘着性組成物の製造時の作業性に問題があった。また、液状ポリブテンも2種類使用することが必要で、この点でも製造作業は煩雑であった。
また、脂環式炭化水素樹脂の使用割合が少なすぎる組成物(比較例5)は溶融粘度が高過ぎ、塗布作業性に問題があった。また脂環式炭化水素樹脂の使用割合が多すぎる配合物(比較例6)は、塗布面が硬すぎるものとなり、そのため粘着力が無く、小生物の捕獲性が劣る。また、溶融時の粘度が低すぎるため、塗布作業時に広がりが大きくなりすぎ形状を保つことが困難であった。
それに対し実施例1、2および3で例示される本発明の粘着性組成物は塗布作業時の作業性と小生物捕獲性能の双方に優れている。また、粘着性組成物の製造時の均一化に要する時間も短く、製造時の作業性にも優れたものである。また、被塗布材料に塗布後の塗布膜も小生物捕獲場所に設置中に流れ出したり、被塗布材料に滲み出して使用不能になったり周りを汚したりすることは無く、塗布膜の保存性も優れたものであった。
On the other hand, Comparative Example 1 in which no alicyclic hydrocarbon resin is blended is excellent in workability at the time of application, but is inferior in adhesive strength. In Comparative Example 2, in which the blending ratio of butyl rubber was increased and the liquid polybutene having a large viscosity was used in combination with the adhesive strength in Examples 1 and 2, the adhesive strength was excellent, but the melt viscosity was large. Inferior workability. Further, Comparative Example 3 using an aliphatic hydrocarbon resin instead of the alicyclic hydrocarbon resin as the hydrocarbon resin is excellent in workability at the time of coating, but is inferior in adhesive strength, and is derived from the resin B. The odor of the sticky material was also strong. Comparative Example 4 is currently marketed and is widely used as an adhesive composition for capturing small organisms, and has an excellent track record in both adhesive strength and coating workability. As is apparent from the table, Examples 1, 2 and 3 have adhesive strength and coating workability which are not inferior to those of Comparative Example 4. Further, in Comparative Example 4, an ultra high molecular weight polyisobutylene rubber is used instead of the butyl rubber of the present application. Therefore, as shown in Table 1, it took a long time until the kneaded product became uniform during the kneading operation, and there was a problem in workability during the production of the adhesive composition. Also, it is necessary to use two types of liquid polybutenes, and the manufacturing work is complicated in this respect as well.
Moreover, the composition (Comparative Example 5) in which the use ratio of the alicyclic hydrocarbon resin is too small has a problem that the melt viscosity is too high and the coating workability is poor. Moreover, the compound (Comparative Example 6) in which the use ratio of the alicyclic hydrocarbon resin is too large is such that the coated surface is too hard. In addition, since the viscosity at the time of melting is too low, the spread becomes too large during the coating operation, and it has been difficult to maintain the shape.
On the other hand, the pressure-sensitive adhesive composition of the present invention exemplified in Examples 1, 2, and 3 is excellent in both workability at the time of coating work and small organism capture performance. In addition, the time required for homogenization during the production of the adhesive composition is short, and the workability during the production is also excellent. In addition, the coating film after coating on the material to be coated does not flow out during installation in the small organism capture place, does not ooze out on the material to be coated, becomes unusable, and does not stain the surroundings, and the coating film can be preserved. It was excellent.

本発明により、ネズミ等のげっ歯小生物に対し優れた捕獲性を有する粘着性組成物を提供できる。また、本発明の小生物捕獲用粘着性組成物は、製造時の作業性に優れていることから経済的に製造可能である。さらに、当該粘着性組成物は塗布作業性に優れていることから、被塗布材料への塗布作業も経済的に実施可能である。
これらのことから、本発明の小生物捕獲用粘着性組成物は、ネズミ等のげっ歯小生物を効率的かつ経済的に駆除することができ、それによりこれらのげっ歯小生物による農産物や食品の被害、さらには鉛管や電灯線の被害を経済的かつ効果的に防止できるものである。
ADVANTAGE OF THE INVENTION By this invention, the adhesive composition which has the capture property outstanding with respect to rodent small organisms, such as a rat, can be provided. Moreover, the adhesive composition for capturing small organisms of the present invention can be economically produced because of its excellent workability during production. Furthermore, since the adhesive composition is excellent in application workability, the application work to the material to be applied can be carried out economically.
From these, the adhesive composition for capturing small organisms of the present invention can efficiently and economically control rodent small organisms such as mice, and thereby produce agricultural products and foods by these rodent small organisms. Damage, as well as damage to lead pipes and power lines can be prevented economically and effectively.

Claims (1)

(A)数平均分子量200 〜1200 の液状ポリブテン70 〜98 質量%、および
(B)メルトインデックスが0.04 〜35の高圧法ポリエチレン1.0〜8.0質量%、
(C)ムーニー粘度ML1+8(125℃)30〜60のブチルゴム1.0〜8.0質量%、および
(D)脂環式炭化水素樹脂5〜29質量%より成る(全体を100質量%とする)ことを特徴とする小生物捕獲用粘着性組成物。
(A) 70-98% by mass of liquid polybutene having a number average molecular weight of 200-1200, and (B) 1.0-8.0% by mass of high-pressure polyethylene having a melt index of 0.04-35,
(C) Mooney viscosity ML 1 + 8 (125 ° C.) 30 to 60 butyl rubber 1.0 to 8.0 mass%, and (D) alicyclic hydrocarbon resin 5 to 29 mass% (total 100 mass) %)), A sticky composition for capturing small organisms.
JP2008050228A 2008-02-29 2008-02-29 Adhesive composition for capturing small creature Pending JP2009203446A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2008050228A JP2009203446A (en) 2008-02-29 2008-02-29 Adhesive composition for capturing small creature
TW098104822A TWI449764B (en) 2008-02-29 2009-02-16 Adhesive composition for small biological trapping
PCT/JP2009/053467 WO2009107687A1 (en) 2008-02-29 2009-02-19 Pressure-sensitive adhesive composition for trapping small organisms
CN2009801066484A CN101959986B (en) 2008-02-29 2009-02-19 Adhesive composition for trapping small organisms

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008050228A JP2009203446A (en) 2008-02-29 2008-02-29 Adhesive composition for capturing small creature

Publications (1)

Publication Number Publication Date
JP2009203446A true JP2009203446A (en) 2009-09-10

Family

ID=41016075

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008050228A Pending JP2009203446A (en) 2008-02-29 2008-02-29 Adhesive composition for capturing small creature

Country Status (4)

Country Link
JP (1) JP2009203446A (en)
CN (1) CN101959986B (en)
TW (1) TWI449764B (en)
WO (1) WO2009107687A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019178272A (en) * 2018-03-30 2019-10-17 積水フーラー株式会社 Hot-melt composition

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102850965B (en) * 2012-08-13 2014-07-23 北京绿叶世纪日化用品有限公司 Binder, preparation method of the binder and insect bonding plate coated with the binder
CN102850966A (en) * 2012-08-13 2013-01-02 北京绿叶世纪日化用品有限公司 Rat glue having attraction effects, preparation method of the rat glue and rat glue plate coated with the rat glue
CN103497711B (en) * 2013-08-07 2015-11-11 佛山力得高科技有限公司 Sticky mouse glue and preparation method thereof
CN103709977B (en) * 2013-12-04 2017-07-11 浙江固特热熔胶有限公司 The efficient Mouse adhering glue of environmental protection and public nuisance free and its production method
EP3601464A4 (en) * 2017-03-31 2020-09-02 3M Innovative Properties Company Adhesive comprising low molecular weight polyisobutylene polymer and styrene isobutylene block copolymer
JP7430059B2 (en) 2019-12-26 2024-02-09 積水フーラー株式会社 hot melt composition

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52154781A (en) * 1976-06-18 1977-12-22 Nitto Electric Ind Co Ltd Vermin adhesive collector
JPS5626968A (en) * 1979-07-13 1981-03-16 Nichiban Co Ltd Adhesive tape for bundling raw vegetable of flower
JPS58180401A (en) * 1982-04-16 1983-10-21 Nippon Oil Co Ltd Adhesive composition for capturing small life
JPS58180402A (en) * 1982-04-16 1983-10-21 Nippon Oil Co Ltd Improved adhesive composition for capturing small life
JPH1081856A (en) * 1996-04-01 1998-03-31 Bridgestone Corp Adhesive tape composition and method for covering roof
JP2000262202A (en) * 1999-03-18 2000-09-26 Nitta Gelatin Inc Sticky composition for trapping small living thing and tool for trapping small living thing
JP2007177105A (en) * 2005-12-28 2007-07-12 Nippon Oil Corp Adhesive for capturing small creature
JP2007177104A (en) * 2005-12-28 2007-07-12 Nippon Oil Corp Adhesive composition for capturing small creature

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH09143443A (en) * 1995-11-22 1997-06-03 Nitto Denko Corp Tacky agent and tacky catching tool

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS52154781A (en) * 1976-06-18 1977-12-22 Nitto Electric Ind Co Ltd Vermin adhesive collector
JPS5626968A (en) * 1979-07-13 1981-03-16 Nichiban Co Ltd Adhesive tape for bundling raw vegetable of flower
JPS58180401A (en) * 1982-04-16 1983-10-21 Nippon Oil Co Ltd Adhesive composition for capturing small life
JPS58180402A (en) * 1982-04-16 1983-10-21 Nippon Oil Co Ltd Improved adhesive composition for capturing small life
JPH1081856A (en) * 1996-04-01 1998-03-31 Bridgestone Corp Adhesive tape composition and method for covering roof
JP2000262202A (en) * 1999-03-18 2000-09-26 Nitta Gelatin Inc Sticky composition for trapping small living thing and tool for trapping small living thing
JP2007177105A (en) * 2005-12-28 2007-07-12 Nippon Oil Corp Adhesive for capturing small creature
JP2007177104A (en) * 2005-12-28 2007-07-12 Nippon Oil Corp Adhesive composition for capturing small creature

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2019178272A (en) * 2018-03-30 2019-10-17 積水フーラー株式会社 Hot-melt composition

Also Published As

Publication number Publication date
TW200936723A (en) 2009-09-01
CN101959986B (en) 2013-10-16
TWI449764B (en) 2014-08-21
WO2009107687A1 (en) 2009-09-03
CN101959986A (en) 2011-01-26

Similar Documents

Publication Publication Date Title
JP2009203446A (en) Adhesive composition for capturing small creature
CN1183218C (en) Hot melt adhesive based on blends of EPR and/or EPDM and semicrystalline olefinic polymers
CN104603222B (en) There is the bonding agent of the binding material blend being made up of acrylic acid and styrene block copolymer
JP6031640B2 (en) Hot melt adhesive
JP4146568B2 (en) Adhesive composition for capturing small organisms and small organism capturing tool using the same
CN107207913A (en) Expandable hot melt gasket seal agent and application thereof
JP4791821B2 (en) Adhesive composition for capturing small organisms
CN104497935A (en) Reactive-type plasticizer-free SIS hot-melt pressure-sensitive adhesive
JP5052086B2 (en) Hot melt adhesive composition for capturing small animals
JP3676079B2 (en) Polymer composition
KR101617468B1 (en) Small animal trapping material
JP5478452B2 (en) Small organism capture material
JP4969102B2 (en) Adhesive for capturing small organisms
JPH0257521B2 (en)
JPH0128722B2 (en)
JP2012082312A (en) Thermoplastic resin water-based dispersion and waterproof film using this
JPS63215784A (en) Tacky agent
JPH11349402A (en) Pressure sensitive adhesive composition for capturing noxious small animal
JP3172763B2 (en) Adhesive emulsion for capturing small organisms
JPH0256321B2 (en)
JPH0446241B2 (en)
JPH01271445A (en) Pressure-sensitive adhesive
JP4766389B2 (en) Hot melt adhesive
JPH10304807A (en) Adhesive composition for capturing harmful, small animal
JP2024083694A (en) Hot melt composition for trapping small animals

Legal Events

Date Code Title Description
RD04 Notification of resignation of power of attorney

Free format text: JAPANESE INTERMEDIATE CODE: A7424

Effective date: 20090724

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20100823

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20120918

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20121109

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20130813